Canonical Allele Identifier: CA448963502

Gene: KAAG1 DCDC2

Linked Data

• MyVariant Identifiers: chr6:g.24357766G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24357538G>A , CM000668.2:g.24357538G>A	GRCh38
NC_000006.11:g.24357766G>A , CM000668.1:g.24357766G>A	GRCh37
NC_000006.10:g.24465745G>A	NCBI36
NG_012829.1:g.5515C>T
NG_012829.2:g.30755C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000274766.2:c.-102G>A (KAAG1)	ENSP00000274766.1:n.-102G>A
ENST00000378454.8:c.213C>T (DCDC2) MANE Select	ENSP00000367715.3:p.Gly71=
ENST00000274766.1:c.-102G>A (KAAG1)	ENSP00000274766.1:n.-102G>A
ENST00000378454.7:c.213C>T (DCDC2)	ENSP00000367715.3:p.Gly71=
ENST00000436313.1:c.116C>T (DCDC2)
NM_001195610.1:c.213C>T (DCDC2)	NP_001182539.1:p.Gly71=
NM_016356.4:c.213C>T (DCDC2)	NP_057440.2:p.Gly71=
NM_181337.3:c.-102G>A (KAAG1)	NP_851854.1:n.-102G>A
NM_016356.5:c.213C>T (DCDC2) MANE Select	NP_057440.2:p.Gly71=
NM_181337.4:c.-102G>A (KAAG1)	NP_851854.1:n.-102G>A
NM_001195610.2:c.213C>T (DCDC2)	NP_001182539.1:p.Gly71=
NR_174942.1:n.636G>A (KAAG1)